FDA Import Refusal 799-1994155-9/11/1 — Sqi Diagnostics Systems Inc.
The FDA refused shipment 799-1994155-9/11/1 from Sqi Diagnostics Systems Inc. (Canada) on Dec 2, 2022. The refused product falls under Devices — COVID-19 TEST HOME COLLECTION KIT DEVICES. Cited charges: 118,3280,508
Refusal details
- Date
- Dec 2, 2022
- Country
- Canada
- Product Category
- Devices
- Product Code
- 83QLW COVID-19 TEST HOME COLLECTION KIT DEVICES
- Charges
- 118,3280,508